MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis
Background. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was...
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2019-01-01
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Series: | Mediators of Inflammation |
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doaj-fc1886544ae944479aa474179b672d602020-11-25T01:13:57ZengHindawi LimitedMediators of Inflammation0962-93511466-18612019-01-01201910.1155/2019/50492455049245MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its PathogenesisSilvia Méndez-Flores0Janette Furuzawa-Carballeda1Gabriela Hernández-Molina2Gustavo Ramírez-Martinez3Nora E. Regino-Zamarripa4Blanca Ortiz-Quintero5Luis Jiménez-Alvarez6Alfredo Cruz-Lagunas7Joaquín Zúñiga8Department of Dermatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoDepartment of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoDepartment of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoDepartment of Biochemistry, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoLaboratory of Immunobiology and Genetics, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, MexicoBackground. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was a cross-sectional study. We included 22 patients with subacute (SCLE) and 20 with discoid (DLE) lesions, and 19 healthy donors (HD). qRT-PCR for miRNA analysis, flow cytometry in peripheral blood, and skin immunohistochemistry were performed to determine the distribution of CD4 T cells and regulatory cells and their correlation with circulating miRNAs. Results. miR-150, miR-1246, miR-21, miR-23b, and miR-146 levels were downregulated in SCLE vs. HD. miR-150, miR-1246, and miR-21 levels were downregulated in DLE vs. HD. Peripheral CD4+/CD25-/IL-4+ cells and CD4+/CD25hi/Foxp3+ were negatively associated with miR-23b, and CD4+/CD25-/IFN-γ+ with miR-1246 in SCLE, whereas CD123+/CD196+/IDO+ cells were positively associated with miR-150 in DLE. In the tissue, CD4+/IL-4+ and CD20+/IL-10+ cells were positively associated with miR-21 and CD4+/IFN-γ+ with miR-31 in SCLE, whereas CD4+/IL-4+ cells were positively associated with miR-150, and CD20+/IL-10+ cells with miR-1246 and miR-146a in DLE. In the SCLE, lower miR-150 levels were correlated with higher CLASI scores. The KEGG pathway enrichment analysis revealed that cell cycle regulation pathways, p53, TGF-β, thyroid hormone, and cancer signaling pathways were shared between miR-21, miR-31, miR-23b, miR-146a, miR-1246, and miR-150. Conclusions. A downregulation of miR-150, miR-1246, and miR-21 in both CLE varieties vs. HD was determined.http://dx.doi.org/10.1155/2019/5049245 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Silvia Méndez-Flores Janette Furuzawa-Carballeda Gabriela Hernández-Molina Gustavo Ramírez-Martinez Nora E. Regino-Zamarripa Blanca Ortiz-Quintero Luis Jiménez-Alvarez Alfredo Cruz-Lagunas Joaquín Zúñiga |
spellingShingle |
Silvia Méndez-Flores Janette Furuzawa-Carballeda Gabriela Hernández-Molina Gustavo Ramírez-Martinez Nora E. Regino-Zamarripa Blanca Ortiz-Quintero Luis Jiménez-Alvarez Alfredo Cruz-Lagunas Joaquín Zúñiga MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis Mediators of Inflammation |
author_facet |
Silvia Méndez-Flores Janette Furuzawa-Carballeda Gabriela Hernández-Molina Gustavo Ramírez-Martinez Nora E. Regino-Zamarripa Blanca Ortiz-Quintero Luis Jiménez-Alvarez Alfredo Cruz-Lagunas Joaquín Zúñiga |
author_sort |
Silvia Méndez-Flores |
title |
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis |
title_short |
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis |
title_full |
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis |
title_fullStr |
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis |
title_full_unstemmed |
MicroRNA Expression in Cutaneous Lupus: A New Window to Understand Its Pathogenesis |
title_sort |
microrna expression in cutaneous lupus: a new window to understand its pathogenesis |
publisher |
Hindawi Limited |
series |
Mediators of Inflammation |
issn |
0962-9351 1466-1861 |
publishDate |
2019-01-01 |
description |
Background. The role of miRNAs in the pathogenesis of cutaneous lupus has not been studied. Objective. It was to assess the levels of a selected panel of circulating miRNAs that could be involved in the regulation of the immune response, inflammation, and fibrosis in cutaneous lupus. Methods. It was a cross-sectional study. We included 22 patients with subacute (SCLE) and 20 with discoid (DLE) lesions, and 19 healthy donors (HD). qRT-PCR for miRNA analysis, flow cytometry in peripheral blood, and skin immunohistochemistry were performed to determine the distribution of CD4 T cells and regulatory cells and their correlation with circulating miRNAs. Results. miR-150, miR-1246, miR-21, miR-23b, and miR-146 levels were downregulated in SCLE vs. HD. miR-150, miR-1246, and miR-21 levels were downregulated in DLE vs. HD. Peripheral CD4+/CD25-/IL-4+ cells and CD4+/CD25hi/Foxp3+ were negatively associated with miR-23b, and CD4+/CD25-/IFN-γ+ with miR-1246 in SCLE, whereas CD123+/CD196+/IDO+ cells were positively associated with miR-150 in DLE. In the tissue, CD4+/IL-4+ and CD20+/IL-10+ cells were positively associated with miR-21 and CD4+/IFN-γ+ with miR-31 in SCLE, whereas CD4+/IL-4+ cells were positively associated with miR-150, and CD20+/IL-10+ cells with miR-1246 and miR-146a in DLE. In the SCLE, lower miR-150 levels were correlated with higher CLASI scores. The KEGG pathway enrichment analysis revealed that cell cycle regulation pathways, p53, TGF-β, thyroid hormone, and cancer signaling pathways were shared between miR-21, miR-31, miR-23b, miR-146a, miR-1246, and miR-150. Conclusions. A downregulation of miR-150, miR-1246, and miR-21 in both CLE varieties vs. HD was determined. |
url |
http://dx.doi.org/10.1155/2019/5049245 |
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